2025-05-09 17:04:16, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_022762 1825 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens required for meiotic nuclear division 5 homolog B (S. cerevisiae) (RMND5B), mRNA. ACCESSION NM_022762 VERSION NM_022762.3 GI:34147687 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 1825) AUTHORS Pope,S.N. and Lee,I.R. TITLE Yeast two-hybrid identification of prostatic proteins interacting with human sex hormone-binding globulin JOURNAL J. Steroid Biochem. Mol. Biol. 94 (1-3), 203-208 (2005) PUBMED 15862967 REFERENCE 2 (bases 1 to 1825) AUTHORS Colland,F., Jacq,X., Trouplin,V., Mougin,C., Groizeleau,C., Hamburger,A., Meil,A., Wojcik,J., Legrain,P. and Gauthier,J.M. TITLE Functional proteomics mapping of a human signaling pathway JOURNAL Genome Res. 14 (7), 1324-1332 (2004) PUBMED 15231748 REFERENCE 3 (bases 1 to 1825) AUTHORS Clark,H.F., Gurney,A.L., Abaya,E., Baker,K., Baldwin,D., Brush,J., Chen,J., Chow,B., Chui,C., Crowley,C., Currell,B., Deuel,B., Dowd,P., Eaton,D., Foster,J., Grimaldi,C., Gu,Q., Hass,P.E., Heldens,S., Huang,A., Kim,H.S., Klimowski,L., Jin,Y., Johnson,S., Lee,J., Lewis,L., Liao,D., Mark,M., Robbie,E., Sanchez,C., Schoenfeld,J., Seshagiri,S., Simmons,L., Singh,J., Smith,V., Stinson,J., Vagts,A., Vandlen,R., Watanabe,C., Wieand,D., Woods,K., Xie,M.H., Yansura,D., Yi,S., Yu,G., Yuan,J., Zhang,M., Zhang,Z., Goddard,A., Wood,W.I., Godowski,P. and Gray,A. TITLE The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment JOURNAL Genome Res. 13 (10), 2265-2270 (2003) PUBMED 12975309 REMARK Erratum:[Genome Res. 2003 Dec;13(12):2759] COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from BC009911.2. On Aug 25, 2003 this sequence version replaced gi:21362097. ##Evidence-Data-START## Transcript exon combination :: BC009911.2, DQ494789.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025082 [ECO:0000348] ##Evidence-Data-END## FEATURES Location/Qualifiers source 1..1825 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="5" /map="5q35.3" gene 1..1825 /gene="RMND5B" /gene_synonym="GID2; GID2B" /note="required for meiotic nuclear division 5 homolog B (S. cerevisiae)" /db_xref="GeneID:64777" /db_xref="HGNC:26181" /db_xref="HPRD:07985" exon 1..28 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 21 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="" /replace="g" /db_xref="dbSNP:200120111" exon 29..168 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" misc_feature 67..69 /gene="RMND5B" /gene_synonym="GID2; GID2B" /note="upstream in-frame stop codon" variation 81 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:115379028" exon 169..319 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" CDS 181..1362 /gene="RMND5B" /gene_synonym="GID2; GID2B" /note="GID complex subunit 2 homolog B" /codon_start=1 /product="protein RMD5 homolog B" /protein_id="NP_073599.2" /db_xref="GI:21362098" /db_xref="CCDS:CCDS4431.1" /db_xref="GeneID:64777" /db_xref="HGNC:26181" /db_xref="HPRD:07985" /translation="
MEQCACVERELDKVLQKFLTYGQHCERSLEELLHYVGQLRAELASAALQGTPLSATLSLVMSQCCRKIKDTVQKLASDHKDIHSSVSRVGKAIDRNFDSEICGVVSDAVWDAREQQQQILQMAIVEHLYQQGMLSVAEELCQESTLNVDLDFKQPFLELNRILEALHEQDLGPALEWAVSHRQRLLELNSSLEFKLHRLHFIRLLAGGPAKQLEALSYARHFQPFARLHQREIQVMMGSLVYLRLGLEKSPYCHLLDSSHWAEICETFTRDACSLLGLSVESPLSVSFASGCVALPVLMNIKAVIEQRQCTGVWNHKDELPIEIELGMKCWYHSVFACPILRQQTSDSNPPIKLICGHVISRDALNKLINGGKLKCPYCPMEQNPADGKRIIF
" misc_feature 526..624 /gene="RMND5B" /gene_synonym="GID2; GID2B" /note="LisH; Region: LisH; cl11662" /db_xref="CDD:199226" misc_feature 643..1077 /gene="RMND5B" /gene_synonym="GID2; GID2B" /note="CTLH/CRA C-terminal to LisH motif domain; Region: CLTH; pfam10607" /db_xref="CDD:204529" misc_feature 646..816 /gene="RMND5B" /gene_synonym="GID2; GID2B" /note="C-terminal to LisH motif; Region: CTLH; smart00668" /db_xref="CDD:128914" misc_feature 811..1092 /gene="RMND5B" /gene_synonym="GID2; GID2B" /note="CT11-RanBPM; Region: CRA; smart00757" /db_xref="CDD:197862" misc_feature 1174..1314 /gene="RMND5B" /gene_synonym="GID2; GID2B" /note="RING-type zinc-finger, LisH dimerisation motif; Region: zf-RING_LisH; pfam13445" /db_xref="CDD:205623" variation 275 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:200634220" variation 285 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:145470822" variation 293 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:148893359" variation 315 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:61749659" exon 320..465 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 325 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:138151996" variation 369 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:374022084" variation 372 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:142558734" variation 392 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:367905156" variation 393 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:144820574" variation 397 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:138845509" variation 420 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="g" /replace="t" /db_xref="dbSNP:371988683" variation 425 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:374366016" exon 466..606 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 484 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="g" /replace="t" /db_xref="dbSNP:201796710" variation 486 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:113477430" variation 493 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:201368537" variation 504 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:200442577" variation 517 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:142045405" variation 518 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:373641380" variation 549 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:377142730" variation 550 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:200672147" variation 552 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:150817259" variation 578 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:369563622" variation 582 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:61751560" variation 585 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:373439937" variation 591 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:111290494" exon 607..707 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 615 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:114916116" variation 622 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:200266214" variation 644 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:369805544" variation 654 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:114810177" variation 661 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:373987956" variation 681 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:141069988" variation 700 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:368471120" variation 705 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:183796218" exon 708..874 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 712 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:144815482" variation 713 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:147930447" variation 714 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:140368602" variation 715 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:201730015" variation 722 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:372202630" variation 746 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:142121381" variation 787 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:376722623" variation 808 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:369617974" variation 810 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:151177853" variation 831 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:140069738" variation 832 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:150309056" variation 859 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:373548331" variation 868 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="c" /db_xref="dbSNP:374441747" variation 871 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:368667116" variation 872 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:371214275" exon 875..1040 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 900 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:146514336" variation 901 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:141123042" variation 910 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:199566204" variation 911 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:144728558" variation 980 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:370172551" variation 981..982 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="" /replace="t" /db_xref="dbSNP:36110411" variation 988 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:138696545" variation 1008 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="g" /replace="t" /db_xref="dbSNP:73804715" variation 1025 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="" /replace="c" /db_xref="dbSNP:35216626" variation 1034 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:139570120" variation 1035 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:148121600" variation 1038 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:373385402" exon 1041..1143 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 1056 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:375864830" variation 1068 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:61751561" variation 1101 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="g" /replace="t" /db_xref="dbSNP:147257025" variation 1102 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:138539788" variation 1114 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="g" /db_xref="dbSNP:199783828" variation 1127 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:200468025" variation 1134 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:200027282" variation 1135 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:370860902" variation 1142 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:143335953" exon 1144..1298 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 1145 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:147500031" variation 1171 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:368322665" variation 1180 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:371621330" variation 1182 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:140065663" variation 1183 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:150042905" variation 1188 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:374576631" variation 1204 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:144493521" variation 1214 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:183827593" variation 1236 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:200423663" variation 1248 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:148439868" variation 1265 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:367694476" variation 1275 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:201505174" exon 1299..1808 /gene="RMND5B" /gene_synonym="GID2; GID2B" /inference="alignment:Splign:1.39.8" variation 1323 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:191806078" variation 1334 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:199910834" variation 1335 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:142488501" variation 1348 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:146424436" variation 1349 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:200559247" variation 1363 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="g" /replace="t" /db_xref="dbSNP:141085294" variation 1376 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:369574896" variation 1394 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:114802481" variation 1438 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="c" /replace="t" /db_xref="dbSNP:376147183" variation 1595 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="a" /replace="g" /db_xref="dbSNP:3812071" variation 1768 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="g" /replace="t" /db_xref="dbSNP:183578460" variation 1774..1775 /gene="RMND5B" /gene_synonym="GID2; GID2B" /replace="" /replace="c" /db_xref="dbSNP:374973170" ORIGIN
gaagccggggccggggctgcggggcgagttgtcggccctgggccgggagctggagtcccagactcataggtcccggcccagcccccgaagagccgcctcagccggggggagttgctcggactcaaacgtccagtcctcgtgcgaccgcgctgggtcggaagtgagcaggctgaggccaccatggagcagtgtgcgtgcgtggagagagagctggacaaggtcctgcagaagttcctgacctacgggcagcactgtgagcggagcctggaggagctgctgcactacgtgggccagctgcgggctgagctggccagcgcagccctccaggggacccctctctcagccaccctctctctggtgatgtcacagtgctgccggaagatcaaagatacggtgcagaaactggcttcggaccataaggacattcacagcagtgtatcccgagtgggcaaagccattgacaggaacttcgactctgagatctgtggtgttgtgtcagatgcggtgtgggacgcgcgggaacagcagcagcagatcctgcagatggccatcgtggaacacctgtatcagcagggcatgctcagcgtggccgaggagctgtgccaggaatcaacgctgaatgtggacttggatttcaagcagcctttcctagagttgaatcgaatcctggaagccctgcacgaacaagacctgggtcctgcgttggaatgggccgtctcccacaggcagcgcctgctggaactcaacagctccctggagttcaagctgcaccgactgcacttcatccgcctcttggcaggaggccccgcgaagcagctggaggccctcagctatgctcggcacttccagccctttgctcggctgcaccagcgggagatccaggtgatgatgggcagcctggtgtacctgcggctgggcttggagaagtcaccctactgccacctgctggacagcagccactgggcagagatctgtgagacctttacccgggacgcctgttccctgctggggctttctgtggagtccccccttagcgtcagctttgcctctggctgtgtggcgctgcctgtgttgatgaacatcaaggctgtgattgagcagcggcagtgcactggggtctggaatcacaaggacgagttaccgattgagattgaactaggcatgaagtgctggtaccactccgtgttcgcttgccccatcctccgccagcagacgtcagattccaaccctcccatcaagctcatctgtggccatgttatctcccgagatgcactcaataagctcattaatggaggaaagctgaagtgtccctactgtcccatggagcagaacccggcagatgggaaacgcatcatattctgattcctacctggaaggaattttgttgaaaggggttttcacctgtgagccttggtctgtctcggtagggtggtcaacttcagtggactgtggttggtttcagagcgcctggctgaggagttccactgaggggagcactggagcagccctttggcagaggctgaggagggagatggaccagcccacgcctggcacctggctccatggcataaggaaagggagatgctggcctctgtgctcctgctgtcttttcctgtttctgtttgcgtttgacttagtagcaaccgacagagtggcaagggatttggtcttcagcagtagacatccttccacccctgccctcagccaagtctcttgctgccatgccaatgctatgtccacccttgcccctcggcccaagagtgtccagcggtggcccacctcttcctcccactacagcctcaacagtaaaaaaaaaaaaaaaaaa
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